Evaluation of medicinal plant extracts against blood-sucking parasites

The present study was based on assessments of the antiparasitic activities to determine the efficacies of acetone, chloroform, ethyl acetate, hexane, and methanol dried leaf, flower, and seed extracts of Cassia auriculata L., Rhinacanthus nasutus KURZ., Solanum torvum Swartz, Terminalia chebula Retz., and Vitex negundo Linn. were tested against larvae of cattle tick Rhipicephalus (Boophilus) microplus Canestrini, 1887 (Acari: Ixodidae), adult of Haemaphysalis bispinosa Neumann, 1897 (Acarina: Ixodidae), hematophagous fly Hippobosca maculata Leach (Diptera: Hippoboscidae), nymph of goat-lice Damalinia caprae Gurlt (Trichodectidae), and adult sheep parasite Paramphistomum cervi Zeder, 1790 (Digenea: Paramphistomatidae). All plant extracts showed moderate parasitic effects after 24 h of exposure at 3,000 ppm; however, the highest parasite mortality was found in leaf ethyl acetate, flower methanol of C. auriculata, leaf and seed methanol of S. torvum, seed acetone of T. chebula, and leaf hexane extracts of V. negundo against the larvae of R. microplus (LC₅₀ = 335.48, 309.21, 297.43, 414.99, 167.20, and 611.67 ppm; LC₉₀ = 1571.58, 1111.82, 950.98, 1243.64, 595.31, and 1875.50 ppm), the leaf and flower methanol of R. nasutus, leaf and seed methanol of S. torvum, and seed methanol extracts of T. chebula against the nymph of D. caprae (LC₅₀ = 119.26,143.10,164.93,140.47, and 155.98 ppm; LC₉₀ = 356.77, 224.08, 546.20, 479.72, and 496.06 ppm), the leaf methanol of R. nasutus, leaf and seed methanol of S.torvum, and seed acetone of T. chebula against the adult of H. bispinosa (LC₅₀ = 333.15, 328.98, 312.28, and 186.46 ppm; LC₉₀ = 1056.07, 955.39, 946.63, and 590.76 ppm), the leaf methanol of C. auriculata, the leaf and flower methanol of R. nasutus, the leaf ethyl acetate of S. torvum against the H. maculata (LC₅₀ = 303.36, 177.21, 204.58, and 211.41 ppm; LC₉₀ = 939.90, 539.39, 599.43, and 651.90 ppm), and the leaf acetone of C. auriculata, the flower methanol of R. nasutus, the seed methanol of S. torvum, and the seed acetone of T. chebula were tested against the adult of P. cervi (LC₅₀ = 180.54, 168.59, 200.89, and 87.08 ppm; LC₉₀ = 597.51, 558.65, 690.37, and 433.85 ppm), respectively. Therefore, this study provides first report on the veterinary parasitic activity of plant extracts from Southern India.     

Evaluation of larvicidal and nymphicidal potential of plant extracts against <Emphasis Type="Italic">Anopheles subpictus</Emphasis> Grassi, <Emphasis Type="Italic">Culex tritaeniorhynchus</Emphasis> Giles and <Emphasis Type="Italic">Aphis gossypii</Emphasis> Glover

The acetone, chloroform, ethyl acetate, hexane and methanol extracts of peel and leaf extracts of Citrus sinensis, Ocimum canum, Ocimum sanctum and Rhinacanthus nasutus were tested against fourth instar larvae of malaria vector, Anopheles subpictus Grassi, Japanese encephalitis vector, Culex tritaeniorhynchus Giles (Diptera: Culicidae) and feeding deterrence to nymphs of cotton pest, Aphis gossypii Glover (Homoptera: Aphididae). The larval and nymph mortality were observed after 24 h of exposure. All extracts showed moderate larvicidal and nymphicidal effects; however, the highest mortality was found in peel chloroform extract of C. sinensis, leaf ethyl acetate extracts of O. canum and O. sanctum and leaf chloroform extract of R. nasutus against the larvae of A. subpictus (LC₅₀ = 58.25, 88.15, 21.67 and 40.46 ppm; LC₉₀ = 298.31, 528.70, 98.34 and 267.20 ppm), peel methanol extract of C. sinensis, leaf methanol extract of O. canum, ethyl acetate extracts of O. sanctum and R. nasutus against the larvae of C. tritaeniorhynchus (LC₅₀ = 38.15, 72.40, 109.12 and 39.32 ppm; LC₉₀ = 184.67, 268.93, 646.62 and 176.39 ppm), peel hexane extract of C. sinensis, leaf methanol extracts of O. canum and R. nasutus and leaf ethyl acetate extract of O. sanctum against the nymph of A. gossypii (LC₅₀ = 162.89, 80.99, 73.27 and 130.19 ppm; LC₉₀ = 595.40, 293.33, 338.74 and 450.90 ppm), respectively. These results suggest that the peel methanol extracts of C. sinensis and O. canum, ethyl acetate leaf extract of O. sanctum and leaf chloroform and ethyl acetate extract of R. nasutus have the potential to be used as an ideal eco-friendly approach for the control of the A. subpictus, C. tritaeniorhynchus and A. gossypii.     

Laboratory study on larvicidal activity of indigenous plant extracts against <Emphasis Type="Italic">Anopheles subpictus</Emphasis> and <Emphasis Type="Italic">Culex tritaeniorhynchus</Emphasis>

Anopheles subpictus and Culex tritaeniorhynchus have developed resistance to various synthetic insecticides, making its control increasingly difficult. Insecticides of botanical origin may serve as suitable alternative biocontrol techniques in the future. The leaf acetone, chloroform, ethyl acetate, hexane, and methanol extracts of Aegle marmelos (Linn.) Correa ex Roxb, Andrographis lineata Wallich ex Nees., Andrographis paniculata (Burm.f.) Wall. ex Nees., Cocculus hirsutus (L.) Diels, Eclipta prostrata L., and Tagetes erecta L. were tested against fourth-instar larvae of malaria vector, A. subpictus Grassi and Japanese encephalitis vector, C. tritaeniorhynchus Giles (Diptera: Culicidae). All plant extracts showed moderate larvicidal effects after 24 h of exposure at 1,000 ppm; however, the highest larval mortality was found in leaf ethyl acetate of A. marmelos, E. prostrata, hexane, methanol of A. paniculata and C. hirsutus against the larvae of A. subpictus (LC₅₀ = 167.00, 78.28, 67.24, 142.83 ppm; LC₉₀ = 588.31, 360.75, 371.91, and 830.01 ppm) and against the larvae of C. tritaeniorhynchus (LC₅₀ = 99.03, 119.89, 88.50, 105.19 ppm; LC₉₀ = 479.23, 564.85, 416.39, and 507.86 ppm), respectively. These results suggest that the leaf hexane extract of A. paniculata and ethyl acetate extract of E. prostrata have the potential to be used as an ideal eco-friendly approach for the control of the A. subpictus and C. tritaeniorhynchus. Therefore, this study provides first report on the mosquito larvicidal activity of plant extracts against vectors from Southern India.     

Laboratory determination of efficacy of indigenous plant extracts for parasites control

The present study was based on assessments of the antiparasitic activities to determine the efficacies of acetone, chloroform, ethyl acetate, hexane, and methanol dried leaf, flower, and seed extracts of Achyranthes aspera L., Anisomeles malabarica (L.) R. Br., Gloriosa superba L., Psidium guajava L., Ricinus communis L., and Solanum trilobatum L. tested against the larvae of cattle tick Rhipicephalus (Boophilus) microplus (Canestrini 1887) (Acari: Ixodidae), sheep internal parasite Paramphistomum cervi (Zeder 1790) (Digenea: Paramphistomatidae) at 2,000 ppm and fourth instar larvae of Anopheles subpictus Grassi and Culex tritaeniorhynchus Giles (Diptera: Culicidae) at 1,000 ppm. All plant extracts showed moderate effects after 24 h of exposure; however, the highest parasite mortality was found in the leaf ethyl acetate extract of A. aspera, leaf methanol extract of A. malabarica, flower methanol extract of G. superba, and leaf methanol extract of R. communis against the larvae of R. microplus (LC₅₀ = 265.33, 95.97, 153.73, and 181.49 ppm; LC₉₀ = 1,130.18, 393.88, 1,794.25, and 1,829.94 ppm); leaf acetone and chloroform of A. malabarica, flower acetone extract of G. superba, and leaf chloroform and methanol of R. communis against the adult of P. cervi (LC₅₀ = 108.07, 106.69, 157.61, 69.44, and 168.24 ppm; LC₉₀ = 521.77, 463.94, 747.02, 256.52, and 809.45 ppm); leaf ethyl acetate extract of A. aspera, leaf chloroform extract of A. malabarica, flower methanol of G. superba, and leaf methanol extract of R. communis against the larvae of A. subpictus (LC₅₀ = 48.83, 135.36, 106.77, and 102.71 ppm; LC₉₀ = 225.36, 527.24, 471.90, and 483.04 ppm); and leaf ethyl acetate extract of A. aspera, leaf chloroform extract of A. malabarica, flower methanol extract of G. superba, and leaf methanol extract of R. communis against the larvae of C. tritaeniorhynchus (LC₅₀ = 68.27, 95.98, 59.51, and 93.94 ppm; LC₉₀ = 306.88, 393.83, 278.99, and 413.27 ppm), respectively. These results suggest that the leaf ethyl acetate extract of A. aspera, leaf acetone and chloroform extract of A. malabarica, flower methanol extract of G. superba, and leaf methanol extract of R. communis have the potential to be used as an ideal eco-friendly approach for the control of the R. microplus, P. cervi, A. subpictus, and C. tritaeniorhynchus. Therefore, this study provides the first report on the larvae and adult parasitic activity of crude solvent extracts, indigenous plants consumed by the natives in southern India.     

Screening for antifeedant and larvicidal activity of plant extracts against <Emphasis Type="Italic">Helicoverpa armigera</Emphasis> (Hübner), <Emphasis Type="Italic">Sylepta derogata</Emphasis> (F.) and <Emphasis Type="Italic">Anopheles stephensi</Emphasis> (Liston)

Plant extracts, especially botanical insecticides, are currently studied more and more because of the possibility of their use in plant protection. Biological activity of five solvent plant extracts were studied using fourth instar larvae of gram pod borer Helicoverpa armigera (Lepidoptera: Noctuidae), cotton leaf roller Sylepta derogata (Lepidoptera: Pyralidae) and malaria vector Anopheles stephensi (Diptera: Culicidae). Antifeedant and larvicidal activity of acetone, chloroform, ethyl acetate, hexane and methanol peel, leaf and flower extracts of Citrus sinensis, Ocimum canum, Ocimum sanctum and Rhinacanthus nasutus were used in this study. During preliminary screening, the extracts were tested at 1,000 ppm concentration. The larval mortality was observed after 24 h of exposure. All extracts showed moderate larvicidal effects; however, the highest larval mortality was found in peel chloroform extract of C. sinensis, flower methanol extract of O. canum against the larvae of H. armigera (LC₅₀ = 65.10,51.78, LC₉₀ = 277.39 and 218.18 ppm), peel methanol extract of C. sinensis, flower ethyl acetate extract of O. canum and leaf acetone extract of O. sanctum against the larvae of S. derogata (LC₅₀ = 20.27,58.21,36.66, LC₉₀ =113.15,285.70 and 668.02 ppm), peel methanol extract of C. sinensis, leaf and flower ethyl acetate extracts of O. canum against the larvae of A. stephensi (LC₅₀ = 95.74,101.53,28.96, LC₉₀ = 303.20,492.43 and 168.05 ppm), respectively. These results suggest that the chloroform and methanol extract of C. sinensis, ethyl acetate flower extracts of O. canum and acetone extract of O. sanctum have the potential to be used as an ideal eco-friendly approach for the control of the agricultural pests H. armigera, S. derogata and medically important vector A. stephensi.     

Synthesis of silver nanoparticles using Nelumbo nucifera leaf extract and its larvicidal activity against malaria and filariasis vectors

The aim of this study was to investigate the larvicidal potential of the hexane, chloroform, ethyl acetate, acetone, methanol, and aqueous leaf extracts of Nelumbo nucifera Gaertn. (Nymphaeaceae) and synthesized silver nanoparticles using aqueous leaf extract against fourth instar larvae of Anopheles subpictus Grassi and Culex quinquefasciatus Say (Diptera: Culicidae). Nanoparticles are being used in many commercial applications. It was found that aqueous silver ions can be reduced by aqueous extract of plant parts to generate extremely stable silver nanoparticles in water. The results recorded from UV–vis spectrum, scanning electron microscopy, X-ray diffraction, and Fourier transform infrared support the biosynthesis and characterization of silver nanoparticles. Larvae were exposed to varying concentrations of plant extracts and synthesized silver nanoparticles for 24 h. All extracts showed moderate larvicidal effects; however, the maximum efficacy was observed in crude methanol, aqueous, and synthesized silver nanoparticles against the larvae of A. subpictus (LC₅₀ = 8.89, 11.82, and 0.69 ppm; LC₉₀ = 28.65, 36.06, and 2.15 ppm) and against the larvae of C. quinquefasciatus (LC₅₀ = 9.51, 13.65, and 1.10 ppm; LC₉₀ = 28.13, 35.83, and 3.59 ppm), respectively. These results suggest that the leaf methanol, aqueous extracts of N. nucifera, and green synthesis of silver nanoparticles have the potential to be used as an ideal eco-friendly approach for the control of the A. subpictus and C. quinquefasciatus. This is the first report on the mosquito larvicidal activity of the plant extracts and synthesized nanoparticles.     

Differential larvicidal efficacy of four species of <Emphasis Type="Italic">Vitex</Emphasis> against <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> larvae

The early fourth instar larvae of Culex quinquefasciatus, reared in the laboratory were used for larvicidal assay with leaf extracts of Vitex negundo, Vitex trifolia, Vitex peduncularis and Vitex altissima. The methanol extracts of the four species possessed varying levels of larvicidal nature. The highest larvicidal activity was found with the extract of V. trifolia (LC₅₀ = 41.41 ppm) followed by V. peduncularis (LC₅₀ = 76.28 ppm), V. altissima (LC₅₀ = 128.04 ppm) and V. negundo (LC₅₀ = 212.57 ppm).     

Evaluation of botanical extracts against Haemaphysalis bispinosa Neumann and Hippobosca maculata Leach

In the current study, in vitro evaluation of crude hexane, chloroform, ethyl acetate, acetone, and methanol extracts of Anisomeles malabarica (L.) R. Br., Gloriosa superba L., Psidium guajava L., Ricinus communis L., and Solanum trilobatum L. exhibited acaricidal and insecticidal activities against the adult of Haemaphysalis bispinosa Neumann (Acarina: Ixodidae) and hematophagous fly Hippobosca maculata Leach (Diptera: Hippoboscidae). All plant extracts showed moderate toxic effect on parasites after 24 h of exposure; the complete inhibition (100%) at the maximum concentration tested (3,000 ppm) was obtained in acetone, methanol, hexane, and chloroform extracts of A. malabarica; methanol, chloroform, and ethyl acetate extracts of G. superba; acetone extract of P. guajava; methanol extract of R. communis; and leaf hexane extract of S. trilobatum; and the lowest inhibition (38%) was recorded for the seed hexane extract of S. trilobatum. The highest parasite dead was found in leaf acetone and methanol extracts of A. malabarica, seed methanol of G. superba, leaf methanol of R. communis against H. bispinosa (LC₅₀ = 466.15, 719.78, 476.06, and 243.87 ppm; LC₉₀ = 1,837.96, 2,014.47, 1,904.36, and 2,692.15 ppm), leaf hexane and chloroform extracts of A. malabarica, seed chloroform and ethyl acetate of G. superba, leaf acetone of P. guajava, leaf methanol of R. communis, and leaf hexane extract of S. trilobatum against H. maculata (LC₅₀ = 495.61, 414.81, 360.02, 479.37, 646.30, 506.13, and 432.77 ppm; LC₉₀ = 1,914.84, 1,956.59, 1,598.54, 1,636.41, 2,192.73, 1,982.66, and 1,872.33 ppm), respectively. These results suggest that the leaf methanol of R. communis, chloroform extracts of A. malabarica, and chloroform extract of G. superba have the potential to be used as an ideal eco-friendly approach for the control of the H. bispinosa and H. maculata. Therefore, this study provides first report on the parasitic activities of plant extracts from Southern India.     

Efficacy of medicinal plant extracts against malarial vector, <Emphasis Type="Italic">Anopheles subpictus</Emphasis> Grassi

Insecticides of botanical origin may serve as suitable alternative biocontrol techniques in the future. The aim of this study was to evaluate the adulticidal activity and adult emergence inhibition (EI) of leaf hexane, chloroform, ethyl acetate, acetone, and methanol extracts of Aegle marmelos (Linn.) Correa ex Roxb, Andrographis lineata Wallich ex Nees., Andrographis paniculata (Burm.f.) Wall. ex Nees., Cocculus hirsutus L. Diels, Eclipta prostrata L., and Tagetes erecta L. tested against malarial vector, Anopheles subpictus Grassi (Diptera: Culicidae). All plant extracts showed moderate adulticidal activity and EI effects after 24 h of exposure at 1,000 ppm; however, the highest adulticidal activity was observed in ethyl acetate extract of A.lineata, chloroform extract of A.paniculata, acetone extract of C.hirsutus, and methanol extract of T.erecta (LD₅₀ = 126.92, 95.82, 109.40, and 89.83 ppm; LD₉₀ = 542.95, 720.82, 459.03, and 607.85 ppm); and effective EI was found in leaf acetone extract of the A. marmelos, ethyl acetate extract of A.lineata, methanol extracts of C. hirsutus, and T.erecta, (EI₅₀ = 128.14, 79.39, 143.97, and 92.82 ppm; EI₉₀ = 713.53, 293.70, 682.72, and 582.59 ppm), respectively, against A. subpictus. These results suggest that the leaf methanol extract of C. hirsutus and T.erecta have the potential to be used as an ideal eco-friendly approach for the control of A. subpictus. Therefore, this study provides first report on the mosquito adulticidal activity and EI of plant extracts against malaria vector.     

Larvicidal, repellent, and ovicidal activity of marine actinobacteria extracts against Culex tritaeniorhynchus and Culex gelidus

The purpose of the present study was to assess the effect of crude extracts of marine actinobacteria on larvicidal, repellent, and ovicidal activities against Culex tritaeniorhynchus and Culex gelidus (Diptera: Culicidae). The early fourth instar larvae of C. tritaeniorhynchus and C. gelidus, reared in the laboratory, were used for larvicidal, ovicidal, and repellent assay with crude extracts of actinobacteria. Saccharomonospora spp. (LK-1), Streptomyces roseiscleroticus (LK-2), and Streptomyces gedanensis (LK-3) were identified as potential biocide producers. Based on the antimicrobial activity, three strains were chosen for larvicidal activity. The marine actinobacterial extracts showed moderate to high larvicidal effects after 24 h of exposure at 1,000 ppm and the highest larval mortality was found in extract of LK-3 (LC₅₀ = 108.08 ppm and LC₉₀ = 609.15 ppm) against the larvae of C. gelidus and (LC₅₀ = 146.24 ppm and LC₉₀ = 762.69 ppm) against the larvae of C. tritaeniorhynchus. Complete protections for 240 min were found in crude extract of LK-2 and LK-3 at 1,000 ppm, against mosquito bites of C. tritaeniorhynchus and C. gelidus, respectively. After 24-h treatment, mean percent hatchability of the ovicidal activity was observed. The percent hatchability was inversely proportional to the concentration of extract and directly proportional to the eggs. Crude extracts of LK-1 and LK-3 showed no hatchability at 1,000 ppm against C. tritaeniorhynchus and C. gelidus, respectively. This is an ideal ecofriendly approach for the control of Japanese encephalitis vectors, C. tritaeniorhynchus and C. gelidus.     

Efficacy of larvicidal botanical extracts against <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> Say (Diptera: Culicidae)

The present study explored the effects of crude leaf acetone, chloroform, hot water, methanol, petroleum ether (60–80°C), and water extracts of Calotropis procera (Ait) R. Br., Canna indica L., Hibiscus rosa-sinensis Linn., Ipomoea carnea Jacq. spp. fistulosa Choisy, and Sarcostemma brevistigma Wight that were selected for investigating larvicidal potential against second and fourth instar larvae of the laboratory-reared mosquito species, Culex quinquefasciatus Say, in which the major lymphatic filariasis was used. All plant extracts showed moderate larvicidal effects after 24 h of exposure at 1,000 ppm; however, the highest larval mortality was found in leaf acetone, chloroform, methanol, and petroleum ether of C. indica (LC₅₀ = 29.62, 59.18, 40.77, and 44.38 ppm; LC₉₀ = 148.55, 267.87, 165.00, and 171.91 ppm) against second instar larvae (LC₅₀ = 121.88, 118.25, 69.76, and 56.31 ppm; LC₉₀ = 624.35, 573.93, 304.27, and 248.24 ppm) and against fourth instar larvae and acetone, hot water, methanol, and petroleum ether extracts of I. carnea (LC₅₀ = 61.17, 41.07, 41.82, and 39.32 ppm; LC₉₀ = 252.91, 142.67, 423.76, and 176.39 ppm) against second instar larvae (LC₅₀ = 145.37, 58.00, 163.81, and 41.75 ppm; LC₉₀ = 573.30, 181.10, 627.38, and 162.63 ppm) and against fourth instar larvae of C. quinquefasciatus, respectively. These results suggest that the acetone, methanol extracts of C. indica and hot water, petroleum ether extracts of I. carnea have the potential to be used as an ideal eco-friendly approach for the control of the major lymphatic filariasis vector, C. quinquefasciatus.     

Evaluation of larvicidal activity of Acalypha alnifolia Klein ex Willd. (Euphorbiaceae) leaf extract against the malarial vector, Anopheles stephensi, dengue vector, Aedes aegypti and Bancroftian filariasis vector, Culex quinquefasciatus (Diptera: Culicidae)

The leaf extract of Acalypha alnifolia with different solvents — hexane, chloroform, ethyl acetate, acetone and methanol — were tested for larvicidal activity against three important mosquitoes such as malarial vector, Anopheles stephensi, dengue vector, Aedes aegypti and Bancroftian filariasis vector, Culex quinquefasciatus. The medicinal plants were collected from the area around Kallar Hills near the Western Ghats, Coimbatore, India. A. alnifolia plant was washed with tap water and shade dried at room temperature. The dried leaves were powdered mechanically using commercial electrical stainless steel blender. The powder 800 g of the leaf material was extract with 2.5 litre of various each organic solvents such as hexane, chloroform, ethyl acetate, acetone, methanol for 8 h using Soxhlet apparatus, and filtered. The crude plant extracts were evaporated to dryness in a rotary vacuum evaporator. The yield of extracts was hexane (8.64 g), chloroform (10.74 g), ethyl acetate (9.14 g), acetone (10.02 g), and methanol (11.43 g). One gram of the each plant residue was dissolved separately in 100 ml of acetone (stock solution) from which different concentrations, i.e., 50, 150, 250, 350 and 450 ppm, was prepared. The hexane, chloroform, ethyl acetate, acetone was moderate considerable mortality; however, the highest larval mortality was methanolic extract observed in three mosquito vectors. The larval mortality was observed after 24 h exposure. No mortality was observed in the control. The early fourth-instar larvae of A. stephensi had values of LC₅₀ = 197.37, 178.75, 164.34, 149.90 and 125.73 ppm and LC₉₀ = 477.60, 459.21, 435.07, 416.20 and 395.50 ppm, respectively. The A. aegypti had values of LC₅₀ = 202.15, 182.58, 160.35, 146.07 and 128.55 ppm and LC₉₀ = 476.57, 460.83, 440.78, 415.38 and 381.67 ppm, respectively. The C. quinquefasciatus had values of LC₅₀ = 198.79, 172.48, 151.06, 140.69 and 127.98 ppm and LC₉₀ = 458.73, 430.66, 418.78, 408.83 and 386.26 ppm, respectively. The results of the leaf extract of A. alnifloia are promising as good larvicidal activity against the mosquito vector, A. stephensi, A. aegypti, C. quinquefasciatus. Therefore, this study provides first report on the larvicidal activities against three species of mosquito vectors of this plant extracts from Southern India.     

Screening for feeding deterrent activity of herbal extracts against the larvae of malaria vector Anopheles subpictus Grassi

This no-choice, laboratory study focuses on the feeding of homogeneous powdered, dried, yeast with different plant extracts on mosquito fourth-instar larvae to determine the effects on their mortality. Screening for antifeedant activity of plant extracts with some known medicinal attributes could lead to the discovery of new agents for vector control. The aim of this study was to investigate the antifeedant activity of crude leaf hexane, ethyl acetate, acetone, and methanol extracts of Andrographis lineata Wallich ex Nees. (Acanthaceae), Anisomeles malabarica (L.) Sims. (Lamiaceae), Argemone mexicana L. (Papaveraceae), Aristolochia bracteolata Lam. (Aristolochiaceae), Chrysanthemum indium L. (Asteraceae), Datura metal L. (Solanaceae), Eclipta prostrata L. (Asteraceae), and Sesbania grandiflora (L.) Pers. (Fibaceae) against the fourth-instar larvae of Anopheles subpictus Grassi (Diptera:Culicidae). All the crude extracts showed antifeedant activity in a dose-dependent manner. The plant extracts exhibited a significant antifeedant activity after 24 and 48 h of exposure; however, the highest larval mortality was found in leaf ethyl acetate extract of A. malabarica, acetone extract E. prostrata, methanol extract of A. lineata, C. indium, and S. grandiflora after 24 h (LC₅₀ = 2.53, 2.82, 2.31, 2.56, and 2.08 mg/mL; LC₉₀ = 6.40, 8.06, 7.45, 6.98, and 6.20 mg/mL), respectively. The hexane extract of A. lineata, D. metal, methanol extract of A. bracteolata and E. prostrata showed larval mortality after 48 h (LC₅₀ = 3.05, 2.11, 3.00, and 2.18 mg/mL; LC₉₀ = 9.06, 6.22, 8.23, and 5.77 mg/mL), respectively. One hundred percent larval mortality was observed in methanol extract of A. lineata, and C. indium after 24 h and the hexane extract of A. lineata and D. metal after 48 h at 10 mg/100 mL. The methanol extracts of A. lineata and C. indium significantly increased larval mortality in comparison to larvae fed with untreated diet. Bacillus thuringiensis subsp. israelensis is widely accepted as a biological pesticide because of its highly specific activity against dipteran insects without adverse effects on other organisms. The feeding deterrent activity of different herbal extracts against the larvae of malaria vector A. subpictus exhibited significantly lower toxicity compare with the bio larvicides, B. thuringiensis. These results suggest that the methanol extract of A. lineata, C. indium, the hexane extract of A. lineata and D. metal have the potential to be used as an ideal eco-friendly approach for the control of the medically important vector A. subpictus. These findings corroborate traditional insecticidal application of selected plants and the results can be extended for the control of mosquitoes.     

Evaluation of larvicidal nature of fleshy fruit wall of Momordica charantia Linn. (family: cucurbitaceae) in the management of mosquitoes

In view of the recently increased interest in developing plant-based insecticides as an alternative to chemical insecticides, this study was undertaken to assess the larvicidal potential of the various fruit wall extracts of Momordica charantia (cucurbitaceae) against two species of mosquito vectors, Anophels stephensi and Culex quinquefasciatus. Among the extracts tested, petroleum ether (LC₅₀ = 27.60; 17.22 ppm and 41.36; 15.62 ppm) extract was found more effective than carbon tetrachloride (LC₅₀ = 49.58; 16.15 ppm and 80.61; 27.64 ppm) and methanol (LC₅₀ = 142.82; 95.98 ppm and 1,057.49; 579.93 ppm) extracts towards anopheline and culicine larvae after 24 and 48 h of exposure respectively. Thus, all fruit wall extracts of M. charantia are toxic to both the larval species. M. charantia may, therefore, act as an effective biolarvicide against mosquitoes in the future.     

Evaluation of indigenous plant extracts against larvae of <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> Say (Diptera: Culicidae)

This study investigates the larvicidal potential of indigenous plant extracts from commonly used medicinal herbs as an environmentally safe measure to control the filarial vector, Culex quinquefasciatus Say (Diptera: Culicidae). The early fourth-instar larvae of C. quinquefasciatus, reared in the laboratory, were used for larvicidal assay with water, hot water, acetone, chloroform, and methanol leaf, stem-bark, and flower extracts of Acacia arabica Willd. Sans, Cedrus deodara Roxb, Hibiscus rosa-sinensis L., Mangifera indica L., Nerium indicum Mill., Nicotiana tabacum Linn., Pongamia pinnata (L.) Pierre, and Solanum nigrum Linn. All plant extracts showed moderate larvicidal effects after 24 h of exposure at 1,000 ppm; however, the highest larval mortality was found in stem-bark hot water, acetone, and methanol extracts of C. deodara (LC₅₀ = 133.85, 141.60, and 95.19 ppm, LC₉₀ = 583.14, 624.19, and 639.99 ppm) and leaf hot water, acetone, methanol, and chloroform extracts of N. tabacum (LC₅₀ = 76.27, 163.81, 83.38, and 105.85 ppm, LC₉₀ = 334.72, 627.38, 709.51, and 524.39 ppm) against the larvae of C. quinquefasciatus, respectively. This is an ideal ecofriendly approach for the control of lymphatic filariasis vector, C. quinquefasciatus.     

Evaluation of medicinal plant extracts against ticks and fluke

The present study was based on assessments of the antiparasitic activities to determine the efficacies of leaf hexane, chloroform, ethyl acetate, acetone and methanol extracts of Aegle marmelos (Linn.) Correa ex Roxb, Andrographis lineata Wallich ex Nees., Andrographis paniculata (Burm.f.) Wallich ex Nees., Cocculus hirsutus (L.) Diels, Eclipta prostrata L., and Tagetes erecta L. against the adult cattle tick Haemaphysalis bispinosa Neumann 1897 (Acarina: Ixodidae), the larvae of Rhipicephalus (Boophilus) microplus Canestrini 1887 (Acari: Ixodidae) and sheep fluke Paramphistomum cervi Zeder 1790 (Digenea: Paramphistomatidae). All plant extracts showed moderate toxic effect on parasites after 24 h of exposure; however, the highest parasitic activity was found in leaf ethyl acetate extract of A. lineata, methanol extract of A. marmelos, A. paniculata, and C. hirsutus against H. bispinosa (LC₅₀ = 395.27, 358.45, 327.21 and 420.50 ppm); ethyl acetate extract of A. paniculata, C. hirsutus, methanol extracts of A. marmelos, A. lineata, and E. prostrata against the larvae of R. microplus (LC₅₀ = 207.70, 258.61, 134.09, 206.00, and 274.33 ppm); hexane extract of A. lineata, ethyl acetate extract of A. paniculata, E. prostrata, acetone extracts of T. erecta, methanol extracts of A. marmelos and C. hirsutus against P. cervi (LC₅₀ = 254.23, 451.17, 425.73, 253.60, 542.71, and 360.17 ppm), respectively. The present study is the first report on the veterinary parasitic activity of plant extracts from Southern India.     

Insecticidal and larvicidal activities of medicinal plant extracts against mosquitoes

In recent years, use of environment friendly and biodegradable natural insecticides of plant origin have received renewed attention as agents for vector control because they are rich in bioactive chemicals, active against a limited number of species including specific target insects, and biodegradable. The present study was carried out to evaluate the adulticidal, repellent, and larvicidal activity of crude hexane, ethyl acetate, and methanol extracts of eight plants, viz. Aristolochia indica L., Cassia angustifolia Vahl, Diospyros melanoxylon Roxb., Dolichos biflorus L., Gymnema sylvestre (Retz) Schult, Justicia procumbens L., Mimosa pudica L., and Zingiber zerumbet L., were tested against adult and early fourth instar larvae of Culex gelidus Theobald and Culex quinquefasciatus Say (Diptera: Culicidae). The effective adult mortality was observed in methanol extract of A. indica, ethyl acetate extract of D. biflorus, and ethyl acetate and hexane extract of Z. zerumbet against C. gelidus and C. quinquefasciatus (LD₅₀ = 37.75, 78.56, 129.44, 86.13, 80.06, 112.42, 53.83, and 46.61; LD₉₀ = 166.83, 379.14, 521.50, 289.83, 328.18, 455.72, 181.15, and 354.50 ppm, respectively). Complete protections for 150 min were found in hexane and methanol extract of A. indica and Z. zerumbet at 1,000 ppm against mosquito bites. The highest larval mortality was found in the hexane extract of Z. zerumbet, ethyl acetate extract of D. biflorus, and methanol extracts of A. indica against C. gelidus (LC₅₀ = 26.48, 33.02, and 12.47 ppm; LC₉₀ = 127.73, 128.79, and 62.33 ppm) and against C. quinquefasciatus (LC₅₀ = 69.18, 34.76, and 25.60 ppm; LC₉₀ = 324.40, 172.78, and 105.52 ppm), respectively, after 24 h. The plant extracts are potential to be used as an ideal eco-friendly approach for the control of the Japanese encephalitis vector, C. gelidus, and lymphatic filariasis vector, C. quinquefasciatus.     

Larvicidal efficacy of five cucurbitaceous plant leaf extracts against mosquito species

Larvicidal activity of crude hexane, ethyl acetate, petroleum ether, acetone, and methanol extracts of the leaf of five species of cucurbitaceous plants, Citrullus colocynthis, Coccinia indica, Cucumis sativus, Momordica charantia, and Trichosanthes anguina, were tested against the early fourth instar larvae of Aedes aegypti L. and Culex quinquefasciatus (Say) (Diptera: Culicidae). The larval mortality was observed after 24 h of exposure. All extracts showed moderate larvicidal effects; however, the highest larval mortality was found in petroleum ether extract of C. colocynthis, methanol extracts of C. indica, C. sativus, M. charantia, and acetone extract of T. anguina against the larvae of A. aegypti (LC₅₀ = 74.57, 309.46, 492.73, 199.14, and 554.20 ppm) and against C. quinquefasciatus (LC₅₀ = 88.24, 377.69, 623.80, 207.61, and 842.34 ppm), respectively. The petroleum ether extract of C. colocynthis and methanol extract of M. charantia were more effective than the other extracts. This is an ideal eco-friendly approach for the control of the dengue vector, A. aegypti, and the lymphatic filariasis vector, C. quinquefasciatus.     

Bioefficacy of larvicdial and pupicidal properties of Carica papaya (Caricaceae) leaf extract and bacterial insecticide, spinosad, against chikungunya vector, Aedes aegypti (Diptera: Culicidae)

The present study was carried out to establish the properties of Carica papaya leaf extract and bacterial insecticide, spinosad on larvicidal and pupicidal activity against the chikungunya vector, Aedes aegypti. The medicinal plants were collected from the area around Bharathiar University, Coimbatore, India. C. papaya leaf was washed with tap water and shade-dried at room temperature. An electrical blender powdered the dried plant materials (leaves). The powder (500 g) of the leaf was extracted with 1.5 l of organic solvents of methanol for 8 h using a Soxhlet apparatus and then filtered. The crude leaf extracts were evaporated to dryness in a rotary vacuum evaporator. The plant extract showed larvicidal and pupicidal effects after 24 h of exposure; however, the highest larval and pupal mortality was found in the leaf extract of methanol C. papaya against the first- to fourth-instar larvae and pupae of values LC₅₀ = I instar was 51.76 ppm, II instar was 61.87 ppm, III instar was 74.07 ppm, and IV instar was 82.18 ppm, and pupae was 440.65 ppm, respectively, and bacterial insecticide, spinosad against the first to fourth instar larvae and pupae of values LC₅₀ = I instar was 51.76 ppm, II instar was 61.87 ppm, III instar was 74.07 ppm, and IV instar was 82.18 ppm, and pupae was 93.44 ppm, respectively. Moreover, combined treatment of values of LC₅₀ = I instar was 55.77 ppm, II instar was 65.77 ppm, III instar was 76.36 ppm, and IV instar was 92.78 ppm, and pupae was 107.62 ppm, respectively. No mortality was observed in the control. The results that the leaves extract of C. papaya and bacterial insecticide, Spinosad is promising as good larvicidal and pupicidal properties of against chikungunya vector, A. aegypti. This is an ideal eco-friendly approach for the control of chikungunya vector, A. aegypti as target species of vector control programs.     

Biolarvicidal compound gymnemagenol isolated from leaf extract of miracle fruit plant, Gymnema sylvestre (Retz) Schult against malaria and filariasis vectors

Owing to the fact that the application of synthetic larvicide has envenomed the surroundings as well as non-target organisms, natural products of plant origin with insecticidal properties have been tried as an indigenous method for the control of a variety of insect pests and vectors in the recent past. Insecticides of plant origin have been extensively used on agricultural pests and, to a very limited extent, against insect vectors of public health importance, which deserve careful and thorough screening. The use of plant extracts for insect control has several appealing features as these are generally more biodegradable, less hazardous and a rich storehouse of chemicals of diverse biological activities. Moreover, herbal sources give a lead for discovering new insecticides. Therefore, biologically active plant materials have attracted considerable interest in mosquito control study in recent times. The crude leaf extracts of Gymnema sylvestre (Retz) Schult (Asclepiadaceae) and purified gymnemagenol compound were studied against the early fourth-instar larvae of Anopheles subpictus Grassi and Culex quinquefasciatus Say (Diptera: Culicidae). In the present study, bioassay-guided fractionation of petroleum ether leaf extract of G. sylvestre led to the separation and identification of gymnemagenol as a potential new antiparasitic compound. Phytochemical analysis of G. sylvestre leaves revealed the presence of active constituents such as carbohydrates, saponins, phytosterols, phenols, flavonoids and tannins. However, cardiac glycosides and phlobatannins are absent in the plant extracts. Quantitative analysis results suggested that saponin (5%) was present in a high concentration followed by tannins (1.0%). The 50 g powder was loaded on silica gel column and eluted with chloroform–methanol–water as eluents. From that, 16 mg pure saponin compound was isolated and analysed by thin layer chromatography using chloroform and methanol as the solvent systems. The structure of the purified triterpenoid fraction was established from infrared (IR), ultraviolet (UV), ¹H nuclear magnetic resonance (NMR), ¹³C NMR and mass spectral data. The carbon skeleton of the compound was obtained by ¹³C NMR spectroscopy. The chemical shift assignments obtained for gymnemagenol from ¹H NMR correspond to the molecular formula C₃₀H₅₀O₄. The compound was identified as 3β, 16β, 28, 29-tetrahydroxyolean-12-ene (gymnemagenol sapogenin). Parasite larvae were exposed to varying concentrations of purified compound gymnemagenol for 24 h. The results suggested that the larval mortality effects of the compound were 28%, 69%, 100% and 31%, 63%, 100% at 6, 12 and 24 h against A. subpictus and C. quinquefasciatus, respectively. In the present study, the per cent mortality were 100, 86, 67, 36, 21 and 100, 78, 59, 38 and 19 observed in the concentrations of 1,000, 500, 250, 125 and 62.75 ppm against the fourth-instar larvae of A. subpitcus and C. quinquefasciatus, respectively. The purified compound gymnemagenol was tested in concentrations of 80, 40, 20, 10 and 5 ppm, and the per cent mortality were 100, 72, 53, 30 and15 against A. subpitcus and 100, 89, 61, 42 and 30 against C. quinquefasciatus, respectively. The larvicidal crude leaf extract of G. sylvestre showed the highest mortality in the concentration of 1,000 ppm against the larvae of A. subpictus (LC₅₀ = 166.28 ppm, r ² = 0.807) and against the larvae of C. quinquefasciatus (LC₅₀ = 186.55 ppm, r ² = 0.884), respectively. The maximum efficacy was observed in gymnemagenol compound with LC₅₀ and r ² values against the larvae of A. subpictus (22.99 ppm, 0.922) and against C. quinquefasciatus (15.92 ppm, 0.854), respectively. The control (distilled water) showed nil mortality in the concurrent assay.